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Recall Observatory FDA recall evidence

Device product

Medtronic O-arm Imaging System Product Usage: image-intensified fluoroscopic x-ray system, mobile

Z-0926-2013

January 31, 2013

Class II

Product summary

Firm
Medtronic Navigation, Inc.
Event
Event 64256
Status
Terminated
Classification
Class II
Quantity
463 units
Official record key
device-enforcement:Z-0926-2013

Official wording

Reason: Potential failure of the braking system that controls the O-arm Imaging System gantry movement in the vertical direction

Code information: Product Catalog Numbers: 9732719, 9732719R, 9733346, 9733346R, BI-700-00027, BI-700-00027R, BI-700-00027-GER, BI-700-00027-GERR, BI-700-00027-100, BI-700-00027-100R, BI-700-00027-120, BI-700-00027-120R, BI-700-00027-230, BI-700-00027-230R Units with serial numbers 101 through 564 and unit 580 are affected. Serial numbers 565 and higher are not affected .

Distribution pattern: Worldwide Distribution - USA Nationwide and the countries of: Canada, AUSTRIA, BELGIUM, BRAZIL, BULGARIA, CHILE, CHINA, CROATIA, CZECH REPUBLIC, DENMARK,FINLAND, FRANCE, GERMANY, GREECE, INDIA, IRELAND, ISRAEL, ITALY, JAPAN ,KOREA, REPUBLIC OF KUWAIT, LEBANON, LIBYAN ARAB JAMAHIRIYA, MEXICO, NETHERLANDS, New Zealand, POLAND, RUSSIAN FEDERATION, SAUDI ARABIA, SINGAPORE, SLOVAKIA, SOUTH AFRICA, SPAIN, SWEDEN, SWITZERLAND, Taiwan(R.O.C.) , THAILAND, TURKEY, UNITED ARAB EMIRATES. and UNITED KINGDOM.

Derived failure modes

  • Unknown

    reason.no_named_rule · v1.0.0

    Potential failure of the braking system that controls the O-arm Imaging System gantry movement in the vertical direction